The 20 Best Andermann Syndrome Doctors Near Me in brick, NJ

Find the Top Andermann Syndrome Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 2 doctor with experience in Andermann Syndrome near brick, NJ. Of these, 2 are Experienced.

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2 providers found
    Experienced in Andermann Syndrome
    Experienced in Andermann Syndrome
    Referral may be required

    Shore Rehabilitation Institute

    425 Jack Martin Boulevard, Ocean University Medical Center, 
    Brick, NJ 
     (0.2 miles away)
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Heikki Uustal is a Physiatrist practicing medicine in Brick, New Jersey. Dr. Uustal is rated as an Experienced provider by MediFind in the treatment of Andermann Syndrome. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Foot Drop, Stroke, Post Polio Syndrome, and Hemiplegia. Dr. Uustal is board certified in American Board Of Physical Medicine And Rehabilitation. Dr. Uustal is currently accepting new patients.

    Experienced in Andermann Syndrome
    Internal Medicine
    Experienced in Andermann Syndrome
    Internal Medicine

    Office

    519 Main Ave, 
    Bay Head, NJ 
     (5.1 miles away)
    Languages Spoken:
    English

    Gail Zimmerman is a primary care provider, practicing in Internal Medicine in Bay Head, New Jersey. Dr. Zimmerman is rated as an Experienced provider by MediFind in the treatment of Andermann Syndrome. Her clinical expertise encompasses Hereditary Sensory Neuropathy Type 1 (HSN1), Septic Arthritis, Tomaculous Neuropathy, and Sensorimotor Polyneuropathy.

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    Last Updated: 09/26/2026

    What is the definition of Andermann Syndrome?

    Andermann syndrome (AS) is a disorder that damages the nerves used for muscle movement and sensation (motor and sensory neuropathy). Agenesis or malformation of the corpus callosum also occurs in most people with this disorder. Signs and symptoms of the disorder include areflexia; hypotonia; amyotrophy; severe progressive weakness and loss of sensation in the limbs; and tremors. Other features may include intellectual disability, seizures, contractures, scoliosis, various psychiatric symptoms, various atypical physical features, and cranial nerve problems that cause facial muscle weakness, ptosis, and difficulty following movements with the eyes (gaze palsy). It is caused by genetic changes in the SLC12A6 gene and is inherited in an autosomal recessive manner.